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Dual-wavelength optical-resolution photoacoustic microscopy for cells with gold nanoparticle bioconjugates in three-dimensional cultures

机译:双波长光学分辨率的三维纳米粒子生物缀有细胞的光学分辨声学显微镜

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Three-dimensional (3D) in vitro models bridge the gap between typical two-dimensional cultures and in vivo conditions. However, conventional optical imaging methods such as confocal microscopy and two-photon microscopy cannot accurately depict cellular processing in 3D models due to limited penetration of photons. We developed a dual-wavelength optical-resolution photoacoustic microscopy (OR-PAM), which provides sufficient penetration depth and spatial resolution, for studying CD8+ cytotoxic T lymphocytes (CTLs) trafficking in an in vitro 3D tumor microenvironment. CTLs play a cardinal role in host defense against tumor. Efficient trafficking of CTLs to the tumor microenvironment is a critical step for cancer immunotherapy. For the proposed system, gold nanospheres and indocyanine green (ICG) have been remarkable choices for contrast agents for photoacoustic signals due to their excellent biocompatibility and high optical absorption. With distinct absorption spectrums, targeted cells with gold nanospheres and ICG respectively can be identified by switching 523-nm and 800-nm laser irradiation. Moreover, we use an x-y galvanometer scanner to obtain high scanning rate. In the developed system, lateral and axial resolutions were designed at 1.6 urn and 5 μm, respectively. We successfully showed that dual-spectral OR-PAM can map either the distribution of CTLs with gold nanospheres at a visible wavelength of 523 nm or the 3D structure of tumor spheres with ICG in an in vitro 3D microenvironment. Our OR-PAM can provide better biological relevant information in cellular interaction and is potential for preclinical screening of anti-cancer drugs.
机译:三维(3D)体外模型桥接典型的二维培养物与体内条件之间的差距。然而,常规的光学成像方法如共聚焦显微镜和双光子显微镜,由于光子的限制,因此不能准确地描绘3D模型中的蜂窝加工。我们开发了双波长光学分辨率光声显微镜(或PAM),其提供足够的穿透深度和空间分辨率,用于研究在体外3D肿瘤微环境中的CD8 +细胞毒性T淋巴细胞(CTL)。 CTLS在对抗肿瘤的主体防御中发挥着红衣主教作用。高效贩运CTL对肿瘤微环境是癌症免疫疗法的关键步骤。对于所提出的系统,由于其优异的生物相容性和高光学吸收,金纳米纳米和吲哚菁绿(ICG)对于光声信号具有显着的选择。通过不同的吸收光谱,可以通过切换523-nm和800nm激光照射来识别具有金纳米球和ICG的靶向细胞。此外,我们使用X-Y电流计扫描仪获得高扫描速率。在开发系统中,横向和轴向分辨率分别设计为1.6瓮和5μm。我们成功地表明,双光谱或PAM可以在523nm的可见波长或肿瘤球体的3D结构中与ICG的3D结构,在体外3D微环境中与肿瘤球体的3D结构的分布映射CTL的分布。我们的或PAM可以提供细胞相互作用的更好的生物相关信息,并且是抗癌药物临床前筛查的潜力。

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